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Home > News & events > News > JDRF-funded researchers develop a genetic test to detect diabetic kidney disease early
Researchers have identified genes that predict the development and progression of diabetic kidney disease, giving us the potential to limit how many people with type 1 experience kidney failure and need invasive treatments such as dialysis.
The researchers, led by JDRF-funded Professor Sam El-Osta, used genetics data from four countries to develop a predictive test for diabetic kidney disease. Team leader of the human epigenetics group, Professor Sam El-Osta from the Department of Diabetes at Monash University, Australia, said: “Our discoveries will influence how we screen people for diabetic kidney disease and improve risk identification, disease prediction and diagnosis.”
Diabetic kidney disease (DKD) is also called diabetic nephropathy because kidneys are made up of lots of small units called nephrons, which filter blood to remove waste. Diabetes can cause damage to the small blood vessels in the kidneys, which in turn damages the nephrons. DKD affects almost a third of people with type 1 diabetes, so it’s an important topic for type 1 researchers.
Clinicians currently use blood and urine tests as well as samples of a person’s kidneys to assess for DKD. But these measures are only sensitive enough to detect DKD once there is already quite a lot of damage. Dr Ishant Khurana, who was part of the international research team in this study, said: “The early stages of diabetic kidney disease are typically without symptoms. We have developed a reliable method that improves predictive risk and diagnostic accuracy.”
Before now, genetic risk studies for DKD have only looked at the genes themselves, but Professor El-Osta’s team studied small tags attached to the genes. These tags are called DNA methylation and can turn genes on or off. So, even if a person has certain genes, these tags can switch them off, so the genes stop working.
The international research team looked at the DNA methylation tags of people with type 1 diabetes from Finland, Denmark, Hong Kong, and Thailand. They found common patterns in the genetics of people from all these countries. People with type 1 diabetes who had fewer DNA tags (less DNA methylation) had a higher risk of developing DKD.
Using this pattern shown in the research data, the researchers developed a genetic test that shows who is most likely to develop DKD. Professor El-Osta said: “This type of genetic testing is going to be the new standard for early detection and DKD care. Our new blood-based test can be readily available and used in remote areas with the added advantage of being more stable than methods measuring other biological parameters.”
This exciting breakthrough means that people with type 1 will be able to tell earlier whether they are at high risk of developing DKD. This will give people more time to learn about DKD and take precautions to slow the progression of their kidney damage. The researchers hope this early detection will help limit how many people with type 1 experience kidney failure and need invasive treatments such as dialysis.
The full study is detailed in a scientific paper published in a journal called Journal of Clinical Investigation. Read the full research study on the early detection of diabetic kidney disease.
The Advanced Technologies & Treatments for Diabetes (ATTD) conference took place in Barcelona this year. There were many topics discussed, from artificial intelligence in type 1 diabetes (T1D) management to how technology can help people with T1D play sports. We will be bringing you three key themes that ran throughout the conference – early detection, cellular cures and disease-modifying therapies.
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You may have seen headlines or social media posts about a new drug called tegoprubart, with some suggesting it could help people with type 1 diabetes (T1D) stop taking insulin.
Researchers funded by Breakthrough T1D in America have used small, electrical implant systems in lab-grown, insulin-producing cells.
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